Search results for "SPECTRA"

showing 10 items of 3542 documents

High-Resolution Spectroscopy and Structure of Osmium Tetroxide. A Benchmark Study on 192OsO4

2012

Osmium tetroxide (OsO(4)) is a heavy tetrahedral molecule that constitutes a benchmark for quantum chemistry calculations. Its favorable spin statistics (due to the zero nuclear spin of oxygen atoms) is such that only A(1) and A(2) (T(d) symmetry) rovibrational levels are allowed, leading to a dense but quite easily resolvable spectrum. We reinvestigate here the ν(1)/ν(3) stretching fundamental (940-980 cm(-1)) dyad region and perform new assignments and effective Hamiltonian parameter fits for the main isotopologue ((192)OsO(4)). We also investigate the ν(2)/ν(4) bending fundamental dyad (300-360 cm(-1)) for the first time and perform a preliminary analysis. New experimental data have been…

ChemistryAnalytical chemistryTetrahedral molecular geometry02 engineering and technologyRotational–vibrational spectroscopy010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesQuantum chemistryMolecular physicsSpectral line0104 chemical sciencesInorganic Chemistrysymbols.namesakesymbolsIsotopologuePhysical and Theoretical Chemistry0210 nano-technologySpectroscopyHamiltonian (quantum mechanics)Spin (physics)Inorganic Chemistry
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Vibrations of a single adsorbed organic molecule: anharmonicity matters!

2010

Vibrational spectroscopy is a powerful tool to identify molecules and to characterise their chemical state. Inelastic electron tunnelling spectroscopy (IETS) combined with scanning tunnelling microscopy (STM) allows the application of vibrational analysis to a single molecule. Up to now, IETS was restricted to small species due to the complexity of vibration spectra for larger molecules. We extend the horizon of IETS for both experiment and theory by measuring the STM-IETS spectra of mercaptopyridine adsorbed on the (111) surface of gold and comparing it to theoretical spectra. Such complex spectra with more than 20 lines can be reliably determined and computed leading to completely new ins…

ChemistryAnharmonicityGeneral Physics and AstronomyInfrared spectroscopySelf-assembled monolayerElectronic structureSpectral linesymbols.namesakeComputational chemistryChemical physicssymbolsMoleculePhysics::Chemical PhysicsPhysical and Theoretical ChemistryRaman spectroscopyQuantum tunnellingPhysical chemistry chemical physics : PCCP
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Dithionite bleaching of thermomechanical pulp: factors having effects on bleaching efficiency

2000

The efficiency of dithionite bleaching of Norway spruce (Picea abies) thermomechanical pulp was studied by applying various multivariate data analysis techniques to analytical data (temperature, pH, ion chromatographic and energy-dispersive X-ray fluorescence data). In addition, modeling the residual sulfur content of bleached pulp by means of diffuse reflectance UV-vis spectral data from laboratory-scale bleaching experiments was attempted. The results indicated that this lignin-preserving bleaching process could be evaluated by means of the analytical data using either PCR or PLS models. These models also indicated that wavelengths below 400 nm should not be used in measuring the pulp bri…

ChemistryApplied MathematicsPulp (paper)Ion chromatographyOrthogonal signal correctionAnalytical chemistryengineering.materialDithioniteAnalytical Chemistrychemistry.chemical_compoundengineeringSulfur contentDiffuse reflectionSpectral dataJournal of Chemometrics
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Tieftemperatur-Remissionsspektren oktaedrisch koordinierter Cu2+ -Ionen im Ligandenfeldbereich / Low temperature reflectance spectra of octahedrally …

1973

Abstract The ligand field reflectance spectra of octahedrally coordinated Cu2+-ions in different host lattices and at different temperature (300 °K - 4 °K) are critically compared. Especially the band shifts with decreasing temperature are analysed with respect to transitions from a dynamical to a static Jahn-Teller effect (macroscopic Jahn -Teller distortion of the lattice). In addition the square planar coordination of Cu2+ is discussed and alternative descriptions in the crystal field formalism and the angular overlap model are given.

ChemistryCu2 ionsAnalytical chemistryGeneral Physics and AstronomyPhysical and Theoretical ChemistryReflectivityMathematical PhysicsSpectral lineZeitschrift für Naturforschung A
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The Triplet Excimer of Naphthalene: A Model System for Triplet−Triplet Interactions and Its Spectral Properties

2011

Basic concepts of triplet excimer formation and triplet−triplet interactions between molecules with conjugated π-systems are investigated by means of ab initio quantum chemical calculations, employing the second-order coupled-cluster method CC2 and the second-order propagator method ADC(2). The naphthalene dimer turns out to be a very fruitful model system for which weak and strong electronic coupling can be identified depending on the mutual arrangement of the monomer moieties. From geometry optimizations in the excited state, we determine binding energies, including solvent effects, and transient absorption spectra. The most stable T1 conformation turns out to be a face-to-face arrangemen…

ChemistryDimerBinding energyIntermolecular forceAb initioPhotochemistryExcimerSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundGeneral EnergyChemical physicsExcited statePhysical and Theoretical ChemistrySolvent effectsThe Journal of Physical Chemistry C
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Recombination processes in rare-earth doped MAl2O4(M = Ca, Sr) persistent phosphors investigated by optically-detected magnetic resonance

2007

Single crystalline MAl 2 O 4 (M = Ca and Sr) persistent phosphors, which are nominally pure or additionally doped with Eu and Nd or Dy, respectively, were investigated for their recombination luminescence (RL) and microwave-induced changes in the RL at low temperatures. The analysis of the optically-detected electron paramagnetic resonance (EPR) spectra, recorded after ultraviolet excitation at 4.2 K, shows that intrinsic donor and acceptor centres are involved in the recombination process. Spectral dependent RL-EPR measurements on undoped CaAl 2 O 4 (CAO) and SrAl 2 O 4 (SAO) show that we deal with only one donor but at least two different acceptors. The g value of the donor is 1.99 in CAO…

ChemistryDopingAnalytical chemistryPhosphorSurfaces and InterfacesCondensed Matter PhysicsAcceptorSpectral lineSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionlawMaterials ChemistryElectrical and Electronic EngineeringLuminescenceElectron paramagnetic resonanceRecombinationExcitationNuclear chemistryphysica status solidi (a)
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Intrinsic luminescence and energy transfer processes in pure and doped YVO 4 crystals

2007

Luminescence properties of nominally pure and neodymium doped YVO4 single crystals have been studied by means of time-resolved luminescence spectroscopy technique. It was detected that, besides the main well-known blue excitonic emission band near 2.8 eV, an additional UV emission band at ∼3.1 eV appears in the spectra of intrinsic luminescence at low temperatures (∼80 K) for all crystals studied. Decay time of the UV band is much faster in comparison with the blue one and the UV band is quenched at temperatures above 150 K. Origin of the UV emission band is discussed. A significant rise front was observed in the relaxation kinetics of Nd3+ emission under band-to-band excitation. The time c…

ChemistryDopingchemistry.chemical_elementAstrophysics::Cosmology and Extragalactic AstrophysicsAtmospheric temperature rangeCondensed Matter PhysicsMolecular physicsNeodymiumSpectral lineIonAtomic physicsLuminescenceSpectroscopyAstrophysics::Galaxy AstrophysicsExcitationphysica status solidi c
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Theoretical Study on the Structures and Electronic Spectra of TCNE2−

2006

Investigations into the charge-separated states and electron-transfer transitions in tetracyanoethylene (TCNE) compiles have recently generated much interest. In this work we present theoretical calculations showing that the most stable structure of the dianion TCNE 2- has D 2d symmetry in vacuum as well as in the solvents dichloromethane and cicetonitrile. By means of the coupled cluster linear response, we compute the vertical electronic spectrum in both the gas phase and solution. The theoreitcal results, are compared to the experimental data and good agreement is achieved.

ChemistryElectronic structureTetracyanoethyleneMolecular physicsAtomic and Molecular Physics and OpticsMolecular electronic transitionSpectral lineSymmetry (physics)chemistry.chemical_compoundCoupled clusterComputational chemistryAb initio quantum chemistry methodsPhysical and Theoretical ChemistrySolvent effectsChemPhysChem
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Ultraviolet luminescence of ScPO4, AlPO4 and GaPO4 crystals.

2013

The luminescence of self-trapped excitons (STEs) was previously observed and described for the case of tetragonal-symmetry ScPO4 single crystals. The subject band in this material is situated in the UV spectral range of ?210?nm or ?5.8?eV. In the present work, we are both expanding this earlier luminescence study and seeking to identify similar luminescence phenomena in other orthophosphate crystals, i.e., AlPO4 and GaPO4. These efforts have proven to be successful?in spite of the structural differences between these materials and ScPO4. Specifically we have found that for AlPO4 and GaPO4, in addition to an ?-quartz-like STE, there is a UV luminescence band that is similar in position and d…

ChemistryExcitonAtmospheric temperature rangeCondensed Matter Physicsmedicine.disease_causePhotochemistryMolecular physicsSpectral lineCrystalPhysics::Space PhysicsmedicineGeneral Materials ScienceSinglet stateTriplet stateLuminescenceUltravioletJournal of physics. Condensed matter : an Institute of Physics journal
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The equilibrium structure of trans-glyoxal from experimental rotational constants and calculated vibration–rotation interaction constants

2003

A total of six high-resolution FT-IR spectra for trans-glyoxal-d2, trans-glyoxal-d1 and trans-glyoxal-13C2 were recorded with a resolution ranging from 0.003 to 0.004 cm−1. By means of a simultaneous ground state combination difference analysis for each of these isotopologues using the Watson Hamiltonian in A-reduction and Ir-representation the ground state rotational constants are obtained. An empirical equilibrium structure is determined for trans-glyoxal using these experimental ground state rotational constants and vibration–rotation interaction constants calculated at the CCSD(T)/cc-pVTZ level of theory. The least-squares fit yields the following structural parameters for trans-glyoxal…

ChemistryGeneral Physics and AstronomyInfrared spectroscopyThermodynamicsSpectral linesymbols.namesakeComputational chemistryKinetic isotope effectsymbolsMoleculeIsotopologueRotational spectroscopyPhysical and Theoretical ChemistryHamiltonian (quantum mechanics)Ground statePhys. Chem. Chem. Phys.
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